• Live Feeds
    • Press Releases
    • Insider Trading
    • FDA Approvals
    • Analyst Ratings
    • Insider Trading
    • SEC filings
    • Market insights
  • Analyst Ratings
  • Alerts
  • Subscriptions
  • AI SuperconnectorNEW
  • Settings
  • RSS Feeds
Quantisnow Logo
  • Live Feeds
    • Press Releases
    • Insider Trading
    • FDA Approvals
    • Analyst Ratings
    • Insider Trading
    • SEC filings
    • Market insights
  • Analyst Ratings
  • Alerts
  • Subscriptions
  • AI SuperconnectorNEW
  • Settings
  • RSS Feeds
PublishGo to AppAI Superconnector
    Quantisnow Logo

    © 2025 quantisnow.com
    Democratizing insights since 2022

    Services
    Live news feedsRSS FeedsAlertsPublish with Us
    Company
    AboutQuantisnow PlusContactJobsAI superconnector for talent & startupsNEWLLM Arena
    Legal
    Terms of usePrivacy policyCookie policy

    Breakthrough Discoveries Unlock $643B Cancer Treatment Market By 2034

    10/8/25 10:58:00 AM ET
    $ANIX
    $CTOR
    $GTBP
    $LXEO
    Biotechnology: Pharmaceutical Preparations
    Health Care
    Biotechnology: Pharmaceutical Preparations
    Health Care
    Get the next $ANIX alert in real time by email

    Equity Insider News Commentary

    Issued on behalf of GT Biopharma, Inc.

    VANCOUVER, BC, Oct. 8, 2025 /PRNewswire/ -- Ohio State researchers recently solved a critical mystery explaining why some cancer immunotherapies fail[1], while a University of Chicago team discovered a common supplement that supercharges immune cells against tumors[2]. These breakthroughs are propelling the global cancer treatment market from $282 billion in 2025 toward $643.5 billion by 2034[3], creating powerful momentum for companies pioneering next-generation approaches including GT Biopharma, Inc. (NASDAQ:GTBP), Lexeo Therapeutics, Inc. (NASDAQ:LXEO), Anixa Biosciences, Inc. (NASDAQ:ANIX), Tempus AI, Inc. (NASDAQ:TEM), and Citius Oncology, Inc. (NASDAQ:CTOR).

     

    Equity Insider Logo (PRNewsfoto/Equity Insider)

     

    Cancer immunotherapy spending alone is forecast to double from $58 billion in 2024 to $120 billion by 2030, according to Mordor Intelligence[4], while over 120 clinical trials are testing RNA-based cancer vaccines that have already reduced melanoma recurrence by 44%[5].

    GT Biopharma, Inc. (NASDAQ:GTBP) is a clinical-stage immunotherapy company making significant progress in its fight against difficult-to-treat cancers. The San Francisco-based biotech announced today that both patients in Cohort 3 of its Phase 1 trial testing GTB-3650 have successfully initiated treatment with no evidence of dose-limiting toxicities or safety concerns to date. The company is now well on track with enrollment and plans to begin dosing patients in Cohort 4 by year-end 2025, with additional data updates anticipated in the first quarter of 2026.

    The Phase 1 trial is testing GTB-3650 in patients with relapsed or refractory CD33-expressing blood cancers, including acute myeloid leukemia (AML) and high-risk myelodysplastic syndrome (MDS). These are patients whose cancers have come back or never responded to standard therapies. The drug works by activating the body's own natural killer cells to attack cancer cells. Patients receive the treatment through continuous infusions in two-week cycles, alternating two weeks on and two weeks off, for up to four months based on how well they're responding.

    Recently, the company successfully moved into Cohort 3 after formal safety reviews of the first two patient groups showed no safety or tolerability problems. What makes the early data particularly interesting is the biomarker evidence. Multiple blood tests from the first four patients showed measurable increases in natural killer cell activity and expansion, and the first patient in Cohort 3 has shown promising evidence of immune activation consistent with levels of activity observed in patients from the previous two lower-dose cohorts. This suggests the drug is doing exactly what it was designed to do—wake up the immune system and direct it against cancer.

    The Phase 1 protocol allows evaluation of GTB-3650 in up to approximately 14 patients, with two patients in each of seven cohorts and doses ranging from 1.25μg/kg/day in Cohort 1 to 100μg/kg/day in Cohort 7. The trial will continue to dose-escalate into the higher ranges anticipated to be necessary to translate heightened immune activation into clinically meaningful evidence of therapeutic activity.

    "We are pleased with the enrollment momentum in our Phase 1 clinical trial evaluating GTB-3650 in cancer patients, which continues to advance on schedule," said Michael Breen, Executive Chairman and CEO of GT Biopharma. "Moving into the third dose cohort after a successful safety review and encouraging early evidence of immunological activity, mark important steps forward in the development of GTB-3650. We look forward to sharing more data later this year to reinforce the ability of our TriKE constructs to activate endogenous NK cells, and the potential for broader utility with other targets to treat solid tumors (GTB-5550) and autoimmune indications (GTB-7550)."

    Beyond blood cancers, GT Biopharma has a second drug candidate moving toward the clinic. GTB-5550 targets a protein called B7H3 that appears in many different types of solid tumors, including breast, lung, ovarian, head and neck, pancreatic, bladder, and prostate cancers. The company expects to submit its application to start human testing of GTB-5550 during the fourth quarter of this year. Unlike many cancer immunotherapies that require lengthy hospital infusions, GTB-5550 is being developed as a simple injection that patients could potentially give themselves at home, similar to insulin shots.

    Both drug candidates are built on GT Biopharma's proprietary TriKE platform, which uses specialized antibody fragments originally discovered in camels and llamas. These molecules are smaller and more stable than traditional antibodies, allowing them to work more effectively. GT Biopharma holds an exclusive worldwide license from the University of Minnesota to develop and commercialize therapies using this technology.

    As of June 30, 2025, GT Biopharma reported cash and cash equivalents of approximately $5.3 million, which management expected would fund operations into the first quarter of 2026.

    CONTINUED… Read this and more news for GT Biopharma, Inc. at: 

    https://equity-insider.com/2025/10/03/the-small-biotech-thats-cracking-the-code-big-pharma-paid-billions-for/

    Lexeo Therapeutics, Inc. (NASDAQ:LXEO) has achieved significant progress with the FDA regarding its LX2006 gene therapy for Friedreich ataxia cardiomyopathy, with the agency indicating openness to pooling Phase I/II data with pivotal study data to support an accelerated approval pathway. Interim clinical data showed participants with abnormal left ventricular mass index achieved an 18% mean reduction at 6 months and 23% mean reduction at 12 months, exceeding the FDA-aligned 10% threshold, while more than 70% of participants demonstrated clinically meaningful improvements across both cardiac and neurologic measures.

    "We are encouraged by our recent dialogue with the FDA on LX2006, and we appreciate the Agency's collaborative spirit as we work to deliver a potentially life-changing therapy to the FA community as efficiently as possible," said R. Nolan Townsend, CEO of Lexeo Therapeutics. "Given the highly compelling data to date that demonstrate clinically meaningful improvements across both cardiac and neurologic measures of FA, we are now pursuing a development strategy that could enable a smaller pivotal study, given the potential to pool data with the ongoing Phase I/II trials, as well as potentially assessing the co-primary endpoint of LVMI earlier than 12 months."

    The company plans to initiate its pivotal study in the first half of 2026, with LX2006 having received Breakthrough Therapy, Regenerative Medicine Advanced Therapy, Orphan Drug and Fast Track designations from the FDA. Treatment with LX2006 has been generally well tolerated with no Grade 3+ serious adverse events to date across 17 participants.

    Anixa Biosciences, Inc. (NASDAQ:ANIX) has completed the final patient visit in its Phase 1 breast cancer vaccine clinical trial, marking a major milestone in the first-in-human evaluation of this novel vaccine invented at Cleveland Clinic. The trial enrolled 35 women across three cohorts: 26 patients with triple-negative breast cancer at risk of recurrence, four in a prevention group with genetic mutations who elected preventive mastectomy, and five receiving the vaccine concurrently with pembrolizumab.

    "While cancer vaccines have historically faced considerable challenges, our approach targets a novel antigen that has not been explored in this setting," said Dr. Amit Kumar, Chairman and CEO of Anixa Biosciences. "We believe this strategy could represent a new paradigm in immuno-oncology, with potential utility in both the prevention and treatment of breast cancer."

    Cleveland Clinic will present full clinical results at the San Antonio Breast Cancer Symposium on December 11, 2025, following submission of the final study report to the U.S. Department of Defense and a Clinical Study Report to the FDA.

    Tempus AI, Inc. (NASDAQ:TEM) subsidiary Ambry Genetics has announced an enhanced breast cancer risk assessment solution through its Ambry CARE Program that integrates breast density into the Tyrer-Cuzick scoring model within electronic health records. The enhancement addresses a critical gap in breast cancer screening, as 93% of women with elevated risk who qualify for breast MRI based on medical and family history never receive one, with the updated tool providing four Tyrer-Cuzick score options aligned with BI-RADS breast density categories to guide screening decisions.

    "Accurately assessing breast cancer risk is key to improving outcomes, but important factors like breast density often get overlooked," said Tom Schoenherr, CEO of Ambry Genetics. "By bringing together Tyrer-Cuzick scoring and breast density right in the EHR, CARE shows how Ambry is making it easier for providers to get actionable insights within their workflow, ultimately helping patients get the care they need."

    A recent study published in the Journal of the National Comprehensive Cancer Network demonstrated that CARE interprets NCCN Guidelines with 99.5% accuracy, reinforcing its reliability as a trusted digital risk assessment tool for clinicians and patients.

    Citius Oncology, Inc. (NASDAQ:CTOR) has established international access to LYMPHIR (denileukin diftitox-cxdl) through Named Patient Programs in Europe, South America and the Middle East, including an exclusive distribution agreement with Integris Pharma S.A. covering Greece, Cyprus, Malta, Bulgaria, Romania, Croatia, Serbia, Albania, Bosnia Herzegovina, Kosovo, Montenegro and North Macedonia. LYMPHIR, approved by the FDA in August 2024 for relapsed or refractory cutaneous T-cell lymphoma after at least one prior systemic therapy, targets an initial U.S. market that management estimates exceeds $400 million and continues to grow.

    "As we prepare to launch LYMPHIR in the U.S., expanding access to international markets through Named Patient Programs is both a patient-driven mission and a strategic opportunity for Citius Oncology," said Leonard Mazur, Chairman and CEO of Citius Oncology and Citius Pharmaceuticals. "These programs allow us to serve patients who urgently need new treatment options, while also giving physicians valuable firsthand experience with LYMPHIR. Our recently signed exclusive distribution agreement with Integris Pharma S.A. further strengthens this effort, establishing a trusted partner to help us bring LYMPHIR to patients across Southern Europe and the Balkans."

    The company is in active discussions with multiple prospective distribution partners across several European Union member states, South America, and select Middle Eastern territories, reflecting its commitment to positioning LYMPHIR for growth in key markets outside the United States. Named Patient Programs provide formally recognized pathways for physicians to request promising therapies on behalf of individual patients when no adequate approved alternatives exist, bridging the gap between clinical trial completion and broad market introduction while LYMPHIR remains available only through country-specific programs where permitted by local law.

    Article Sources: https://equity-insider.com/2025/10/03/the-small-biotech-thats-cracking-the-code-big-pharma-paid-billions-for/

    Logo: https://mma.prnewswire.com/media/2644233/Equity_Insider_Logo.jpg

    CONTACT:

    Equity Insider

    [email protected]

    (604) 265-2873

    DISCLAIMER: Nothing in this publication should be considered as personalized financial advice. We are not licensed under securities laws to address your particular financial situation. No communication by our employees to you should be deemed as personalized financial advice. Please consult a licensed financial advisor before making any investment decision. This is a paid advertisement and is neither an offer nor recommendation to buy or sell any security. We hold no investment licenses and are thus neither licensed nor qualified to provide investment advice. The content in this report or email is not provided to any individual with a view toward their individual circumstances. This article is being distributed by Equity Insider on behalf of Market IQ Media Group Inc. ("MIQ"). MIQ has been paid a fee for GT Biopharma, Inc. advertising and digital media from Creative Digital Media Group ("CDMG"). There may be 3rd parties who may have shares of GT Biopharma, Inc., and may liquidate their shares which could have a negative effect on the price of the stock. This compensation constitutes a conflict of interest as to our ability to remain objective in our communication regarding the profiled company. Because of this conflict, individuals are strongly encouraged to not use this publication as the basis for any investment decision. The owner/operator of MIQ/BAY does not own any shares of GT Biopharma, Inc. but reserve the right to buy and sell, and will buy and sell shares of GT Biopharma, Inc. at any time without any further notice commencing immediately and ongoing. We also expect further compensation as an ongoing digital media effort to increase visibility for the company, no further notice will be given, but let this disclaimer serve as notice that all material, including this article, which is disseminated by MIQ has been approved on behalf of GT Biopharma, Inc. by CDMG; this is a paid advertisement, we currently own shares of GT Biopharma, Inc. and will buy and sell shares of the company in the open market, or through private placements, and/or other investment vehicles. While all information is believed to be reliable, it is not guaranteed by us to be accurate. Individuals should assume that all information contained in our newsletter is not trustworthy unless verified by their own independent research. Also, because events and circumstances frequently do not occur as expected, there will likely be differences between the any predictions and actual results. Always consult a licensed investment professional before making any investment decision. Be extremely careful, investing in securities carries a high degree of risk; you may likely lose some or all of the investment.

    SOURCES CITED:

    1. https://www.sciencedaily.com/releases/2025/10/251003033909.htm
    2. https://www.sciencedaily.com/releases/2025/10/251001092214.htm 
    3. https://www.openpr.com/news/4212200/cancer-treatment-market-to-surpass-usd-643-5-billion-by-2034 
    4. https://www.mordorintelligence.com/industry-reports/cancer-therapy-market 
    5. https://pmc.ncbi.nlm.nih.gov/articles/PMC12153701/ 

    Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/breakthrough-discoveries-unlock-643b-cancer-treatment-market-by-2034-302578496.html

    SOURCE Equity Insider

    Get the next $ANIX alert in real time by email

    Crush Q3 2025 with the Best AI Superconnector

    Stay ahead of the competition with Standout.work - your AI-powered talent-to-startup matching platform.

    AI-Powered Inbox
    Context-aware email replies
    Strategic Decision Support
    Get Started with Standout.work

    Recent Analyst Ratings for
    $ANIX
    $CTOR
    $GTBP
    $LXEO

    CompanyDatePrice TargetRatingAnalyst
    Citius Oncology Inc.
    $CTOR
    9/23/2025$6.00Hold → Buy
    Maxim Group
    Tempus AI Inc.
    $TEM
    9/2/2025$90.00Buy
    H.C. Wainwright
    Lexeo Therapeutics Inc.
    $LXEO
    7/31/2025$20.00Outperform
    Oppenheimer
    Tempus AI Inc.
    $TEM
    4/21/2025$60.00Buy
    BTIG Research
    Anixa Biosciences Inc.
    $ANIX
    3/21/2025$10.00Buy
    Maxim Group
    Tempus AI Inc.
    $TEM
    2/25/2025$50.00 → $55.00Overweight → Neutral
    Analyst
    Tempus AI Inc.
    $TEM
    2/12/2025Outperform → Mkt Perform
    William Blair
    Tempus AI Inc.
    $TEM
    2/5/2025$58.00 → $74.00Buy
    TD Cowen
    More analyst ratings

    $ANIX
    $CTOR
    $GTBP
    $LXEO
    SEC Filings

    View All

    Lexeo Therapeutics Inc. filed SEC Form 8-K: Regulation FD Disclosure, Other Events, Financial Statements and Exhibits

    8-K - Lexeo Therapeutics, Inc. (0001907108) (Filer)

    10/7/25 6:03:59 AM ET
    $LXEO
    Biotechnology: Biological Products (No Diagnostic Substances)
    Health Care

    SEC Form EFFECT filed by Anixa Biosciences Inc.

    EFFECT - Anixa Biosciences Inc (0000715446) (Filer)

    10/1/25 12:15:26 AM ET
    $ANIX
    Biotechnology: Pharmaceutical Preparations
    Health Care

    SEC Form DEF 14A filed by Citius Oncology Inc.

    DEF 14A - CITIUS ONCOLOGY, INC. (0001851484) (Filer)

    9/26/25 4:30:39 PM ET
    $CTOR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $ANIX
    $CTOR
    $GTBP
    $LXEO
    Insider Purchases

    Insider purchases reveal critical bullish sentiment about the company from key stakeholders. See them live in this feed.

    View All

    Director Titterton Lewis H Jr bought $30,800 worth of shares (10,000 units at $3.08), increasing direct ownership by 1% to 953,334 units (SEC Form 4)

    4 - Anixa Biosciences Inc (0000715446) (Issuer)

    8/4/25 9:00:05 AM ET
    $ANIX
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Chief Executive Officer Kumar Amit bought $15,800 worth of shares (5,000 units at $3.16), increasing direct ownership by 0.87% to 579,925 units (SEC Form 4)

    4 - Anixa Biosciences Inc (0000715446) (Issuer)

    7/31/25 9:00:04 AM ET
    $ANIX
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Director Baskies Arnold M bought $16,950 worth of shares (5,000 units at $3.39), increasing direct ownership by 4% to 125,000 units (SEC Form 4)

    4 - Anixa Biosciences Inc (0000715446) (Issuer)

    7/21/25 8:30:06 AM ET
    $ANIX
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $ANIX
    $CTOR
    $GTBP
    $LXEO
    Insider Trading

    Insider transactions reveal critical sentiment about the company from key stakeholders. See them live in this feed.

    View All

    Chief Operating Officer Fukushima Ryan sold $461,606 worth of shares (5,000 units at $92.32) (SEC Form 4)

    4 - Tempus AI, Inc. (0001717115) (Issuer)

    10/8/25 4:15:07 PM ET
    $TEM
    Computer Software: Programming Data Processing
    Technology

    CEO and Chairman Lefkofsky Eric P sold $25,457,014 worth of shares (332,500 units at $76.56) (SEC Form 4)

    4 - Tempus AI, Inc. (0001717115) (Issuer)

    9/29/25 4:33:00 PM ET
    $TEM
    Computer Software: Programming Data Processing
    Technology

    Chief Medical Officer Czuczman Myron was granted 825,000 shares (SEC Form 4)

    4 - CITIUS ONCOLOGY, INC. (0001851484) (Issuer)

    9/23/25 4:10:20 PM ET
    $CTOR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $ANIX
    $CTOR
    $GTBP
    $LXEO
    Analyst Ratings

    Analyst ratings in real time. Analyst ratings have a very high impact on the underlying stock. See them live in this feed.

    View All

    Citius Oncology upgraded by Maxim Group with a new price target

    Maxim Group upgraded Citius Oncology from Hold to Buy and set a new price target of $6.00

    9/23/25 7:47:11 AM ET
    $CTOR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    H.C. Wainwright initiated coverage on Tempus AI with a new price target

    H.C. Wainwright initiated coverage of Tempus AI with a rating of Buy and set a new price target of $90.00

    9/2/25 8:40:58 AM ET
    $TEM
    Computer Software: Programming Data Processing
    Technology

    Oppenheimer initiated coverage on Lexeo Therapeutics with a new price target

    Oppenheimer initiated coverage of Lexeo Therapeutics with a rating of Outperform and set a new price target of $20.00

    7/31/25 7:37:07 AM ET
    $LXEO
    Biotechnology: Biological Products (No Diagnostic Substances)
    Health Care

    $ANIX
    $CTOR
    $GTBP
    $LXEO
    Press Releases

    Fastest customizable press release news feed in the world

    View All

    Breakthrough Discoveries Unlock $643B Cancer Treatment Market By 2034

    Equity Insider News Commentary Issued on behalf of GT Biopharma, Inc. VANCOUVER, BC, Oct. 8, 2025 /PRNewswire/ -- Ohio State researchers recently solved a critical mystery explaining why some cancer immunotherapies fail[1], while a University of Chicago team discovered a common supplement that supercharges immune cells against tumors[2]. These breakthroughs are propelling the global cancer treatment market from $282 billion in 2025 toward $643.5 billion by 2034[3], creating powerful momentum for companies pioneering next-generation approaches including GT Biopharma, Inc. (NASDAQ:GTBP), Lexeo Therapeutics, Inc. (NASDAQ:LXEO), Anixa Biosciences, Inc. (NASDAQ:ANIX), Tempus AI, Inc. (NASDAQ:TEM)

    10/8/25 10:58:00 AM ET
    $ANIX
    $CTOR
    $GTBP
    Biotechnology: Pharmaceutical Preparations
    Health Care
    Biotechnology: Biological Products (No Diagnostic Substances)
    Computer Software: Programming Data Processing

    GT Biopharma Provides Enrollment Update on GTB-3650 Phase 1 Trial in Patients with Relapsed or Refractory (r/r) CD33 Expressing Hematologic Malignancies

    The Company is well on track with Phase 1 enrollment now that both patients in Cohort 3 have successfully initiated treatment with no evidence of dose-limiting toxicities or tolerability concerns to date The first patient in Cohort 3 has shown promising evidence of immune activation consistent with levels of activity observed in patients from the previous two lower-dose cohorts; additional update anticipated by year-end Upon successful completion of the Cohort 3 safety assessment, the trial will continue to dose escalate with initiation of Cohort 4 dosing planned by year-end 2025, and flexibility to dose up to 7 cohorts if necessary; additional data updates anticipated in Q1 2026 SAN FRAN

    10/8/25 9:00:00 AM ET
    $GTBP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Citius Oncology Establishes International Access to LYMPHIR™ via Named Patient Programs in Southern Europe

    Exclusive relationship through Named Patient Programs establishes footprint in Greece, Cyprus and additional Balkan countries CRANFORD, N.J., Oct. 7, 2025 /PRNewswire/ -- Citius Oncology, Inc. ("Citius Oncology" or the "Company") (NASDAQ:CTOR), a specialty biopharmaceutical company focused on the development and commercialization of novel targeted oncology therapies today announced it is actively engaging with regional distribution partners to make LYMPHIR™ (denileukin diftitox-cxdl) available to eligible patients through country-specific Named Patient Programs (NPPs) in Europe, South America and the Middle East. As part of its NPP strategy, Citius has entered into an exclusive distribution

    10/7/25 8:47:00 AM ET
    $CTOR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $ANIX
    $CTOR
    $GTBP
    $LXEO
    Leadership Updates

    Live Leadership Updates

    View All

    Amid NCI Budget Fears, Emerging Oncology Stocks Gain Attention

    Equity Insider News CommentaryIssued on behalf of Oncolytics Biotech Inc. VANCOUVER, BC, July 8, 2025 /PRNewswire/ -- Equity Insider News Commentary – As cancer rates climb and drug costs continue to soar, pressure is mounting on the private sector to drive innovation. Now, cancer experts are alarmed over a "gut wrenching" plan from the U.S. government to cut nearly 40% of National Cancer Institute funding, even as the price of oncology treatments pushes new limits—raising urgent concerns about access and affordability. In this shifting landscape, investors are turning their attention to a new wave of biotechs and specialty care providers developing breakthrough therapies and smarter care mo

    7/8/25 10:25:00 AM ET
    $CELC
    $CTOR
    $EXEL
    Medical Specialities
    Health Care
    Biotechnology: Pharmaceutical Preparations
    Biotechnology: Biological Products (No Diagnostic Substances)

    The $900 Billion Question: Who Will Deliver the Next Cancer Breakthrough?

    USA News Group News CommentaryIssued on behalf of Oncolytics Biotech Inc. VANCOUVER, BC, June 26, 2025 /PRNewswire/ -- USA News Group News Commentary – With analysts forecasting the global oncology drug market to surpass US$900 billion by 2034, investor interest in cancer-focused biotechs is rapidly intensifying. ResearchAndMarkets and Vision Research Reports both point to strong double-digit growth, citing surging demand for next-gen diagnostics and immunotherapies. Yet even as market potential grows, the U.S. public health sector is facing potential setbacks. Budget proposals suggest National Cancer Institute (NCI) funding could be slashed by up to 40%, while Bloomberg highlights concerns 

    6/26/25 11:44:00 AM ET
    $ADCT
    $CTOR
    $ONCY
    Biotechnology: Pharmaceutical Preparations
    Health Care

    GT Biopharma Appoints New Member to its Board of Directors

    SAN FRANCISCO, CALIFORNIA, June 13, 2025 (GLOBE NEWSWIRE) -- GT Biopharma, Inc. (the "Company") (NASDAQ:GTBP), a clinical stage immuno-oncology company focused on developing innovative therapeutics based on the Company's proprietary TriKE® natural killer (NK) cell engager platform, today announced the appointment of David C. Mun-Gavin to its Board of Directors. "We are very pleased to welcome David to the Board of Directors. David is an experienced senior executive with global connections and a proven track record of success in working with corporate management teams," said Michael Breen, Executive Chairman and Chief Executive Officer of GT Biopharma. "His guidance and perspective will be

    6/13/25 9:00:00 AM ET
    $GTBP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $ANIX
    $CTOR
    $GTBP
    $LXEO
    Financials

    Live finance-specific insights

    View All

    Tempus Announces the Acquisition of Paige

    Paige's strong foundation in pathology and AI is rooted in its proprietary dataset of almost 7 million digitized pathology slides that are clinically annotated Tempus AI, Inc. (NASDAQ:TEM), a technology company leading the adoption of AI to advance precision medicine, today announced the acquisition of Paige, an AI company specializing in digital pathology. The acquisition allows Tempus to grow its dataset, expand its experienced technical team, and establish a strong footprint in digital pathology with an industry leading technology portfolio. Founded in 2017, Paige has developed and deployed several AI applications, including the first FDA-cleared AI application in pathology, allowin

    8/22/25 9:20:00 AM ET
    $TEM
    Computer Software: Programming Data Processing
    Technology

    Tempus to Report Second Quarter 2025 Financial Results on August 8

    Tempus AI, Inc. (NASDAQ:TEM), a leader in artificial intelligence and precision medicine, today announced they will report financial results for the second quarter of 2025 on Friday, August 8, 2025. The company will hold the earnings conference call at 8:00 a.m. ET. The company's quarterly earnings will be released the same day. The call will feature Tempus Founder and CEO, Eric Lefkofsky, and Chief Financial Officer, Jim Rogers. The live audio webcast will be accessible through the events page of Tempus' Investor Relations website. Alternatively, the call can be accessed via the following: Conference ID: 7005219 Domestic Dial-in Number: (800) 715-9871 International Dial-in Numbe

    7/22/25 8:30:00 AM ET
    $TEM
    Computer Software: Programming Data Processing
    Technology

    Tempus Reports First Quarter 2025 Results

    Tempus AI, Inc. (NASDAQ:TEM), a technology company leading the adoption of AI to advance precision medicine and patient care, today reported financial results for the quarter ended March 31, 2025. Revenue increased 75.4% year-over-year to $255.7 million in the first quarter of 2025 Quarterly gross profit increased 99.8% year-over-year, reaching $155.2 million with continued gross margin improvement in both Genomics and Data and services Announced multi-year, strategic collaborations with AstraZeneca and Pathos to work together to build the largest multimodal foundation model in oncology, resulting in additional $200.0 million in data licensing and model development fees over the next

    5/6/25 4:01:00 PM ET
    $TEM
    Computer Software: Programming Data Processing
    Technology

    $ANIX
    $CTOR
    $GTBP
    $LXEO
    Large Ownership Changes

    This live feed shows all institutional transactions in real time.

    View All

    Amendment: SEC Form SC 13G/A filed by Lexeo Therapeutics Inc.

    SC 13G/A - Lexeo Therapeutics, Inc. (0001907108) (Subject)

    11/14/24 5:49:30 PM ET
    $LXEO
    Biotechnology: Biological Products (No Diagnostic Substances)
    Health Care

    Amendment: SEC Form SC 13G/A filed by Lexeo Therapeutics Inc.

    SC 13G/A - Lexeo Therapeutics, Inc. (0001907108) (Subject)

    11/14/24 4:45:58 PM ET
    $LXEO
    Biotechnology: Biological Products (No Diagnostic Substances)
    Health Care

    Amendment: SEC Form SC 13G/A filed by Lexeo Therapeutics Inc.

    SC 13G/A - Lexeo Therapeutics, Inc. (0001907108) (Subject)

    11/14/24 12:32:15 PM ET
    $LXEO
    Biotechnology: Biological Products (No Diagnostic Substances)
    Health Care